Çѱ¹ ÆÄ·º¼¿ÁÖ½Äȸ»çÀº ¹Ì±¹ Boston¿¡ º»»ç¸¦ µÎ°í ÀÖ´Â »ý¸í°úÇÐ °ü·Ãȸ»çÀÔ´Ï´Ù. ¹Ì±¹ º»»ç ÆÄ·º¼¿Àº ¼³¸³µÈ Áö 30³âÀÌ µÇ¾úÀ¸¸ç, ÇöÀç ¹Ì±¹ ³ª½º´Ú¿¡ »óÀåµÇ¾î ÀÖ´Â global CRO ȸ»çÀÔ´Ï´Ù. ȸ»ç´Â Çѱ¹¿¡¼ 2000³â ¼³¸³µÇ¾úÀ¸¸ç °è¼Ó ¼ºÀåÁßÀΠȸ»çÀÔ´Ï´Ù.
Çѱ¹ ÆÄ·º¼¿¿¡¼ ÀÓ»ó½ÃÇèÀ» ´ã´çÇÒ ¿ª·® ÀÖ°í ÁøÃëÀûÀÎ CRA/Sr.CRA¸¦ ä¿ëÇÏ°í ÀÖ½À´Ï´Ù. Major ´Ù±¹Àû CRO ȸ»ç¿¡¼ ÀÓ»ó Àü¹®ÀÎÀ¸·Î ¼ºÀåÇÏ°íÀÚ ÇÏ´Â ¿©·¯ºÐÀÇ µµÀüÀ» ±â´Ù¸³´Ï´Ù.
´ã´ç ¾÷¹« (Key Job Description)
- Perform all clinical monitoring / site management activities for assigned projects in accordance with PAREXEL¡¯s SOPs.
- Responsible for achieving and maintaining high site performance, managing clinical monitoring activities which includes the ownership of investigator sites, the selection of investigator/sites, collating Regulatory Documentation, initiating and monitoring of sites, performing site documentation verification, data collection and drug accountability in accordance with ICH GCP guidelines.
- Maintain appropriate communication with key internal and external parties.
- Perform site facilities inspection
- Attend audits / Regulatory Inspection if requested
°øÅëÀÚ°Ý ¿ä°Ç (Minimum requirement)
- Àü°ø: ¾àÇÐ/°£È£ÇÐ/ÀÚ¿¬°è ÇлçÇÐÀ§ ¼ÒÁöÀÚ ¿ì´ë
- ¿µ¾î: ¿µ¾î·Î ¾÷¹«¼öÇà°¡´É ÀÚ
- Global Study À¯ °æÇèÀÚ
- CRA °æ·Â ÃÖ¼Ò 1³â ÀÌ»óÀÎÀÚ
- Ä¿¹Â´ÏÄÉÀÌ¼Ç ½ºÅ³
Áö¿ø ¹æ¹ý(How to apply)
¾Æ·¡ e-mail·Î ¿µ¹® À̷¼¸¦ MS word file·Î ¼ÛºÎ. ¸ÞÀÏ Á¦¸ñ¿¡ Áö¿øÇÏ´Â position ±âÀç. À̷¼¿¡´Â ÀÓ»ó°ü·Ã °æ·ÂÀ» ÀÚ¼¼È÷ ±â¼ú. Ashley.noh@parexel.com
Á÷¾÷Á¤º¸Á¦°ø»ç¾÷½Å°í¹øÈ£ J150002023003